Allele Registry

Canonical Allele Identifier: PA117998

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000006540

ClinVar Variation:

6165

HGVS (amino-acid)	Matching Registered Transcripts
NP_004319.1:p.Arg155Pro	CA117994 NM_004328.5:c.464G>C